HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2191766Generated: October 26, 2026
Toluene → Tert-butyl 2-(4-fluoroanilino)-4-(2-isopropoxyphenyl)benzoate
https://huagongshe.com/reaction/2191766
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Toluene | HCID 1140 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | 2-Isopropoxyphenylboronic acid | HCID 5084099 | — |
| Reactant | Tert-butyl 4-bromo-2-(4-fluoroanilino)benzoate | HCID 68956988 | — |
| Catalyst | HCID 178418397 | HCID 178418397 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | Tert-butyl 2-(4-fluoroanilino)-4-(2-isopropoxyphenyl)benzoate | HCID 68964024 | — |
Reaction Steps
To toluene 1.6 mL solution of tert-butyl 4-bromo-2-(4-fluoroanilino)benzoate 70 mg were added ethanol 0.60 mL, water 0.30 mL, 2-isopropoxyphenylboronic acid 0.048 mL, sodium hydrogen carbonate 48 mg and tetrakis(triphenylphosphine)palladium(0) 11 mg at room temperature, and it was heated and refluxed for 6 hours. After the reaction mixture was cooled to room temperature, ethyl acetate and water were added to it. The organic layer was separated and collected,dried over anhydrous magnesium sulfate after washing with saturated sodium chloride aqueous solution, and the solvent was removed under reduced pressure. The obtained residue was refined by silica gel column chromatography [Trikonex company, Flash Tube 2008, eluent; hexane:ethyl acetate=5:1] to give tert-butyl 2-(4-fluoroanilino)-4-(2-isopropoxyphenyl)benzoate.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08327467B2 |
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| Source dataset | uspto-grants-2012_12 |
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| ORD ID | ord-2646f07864eb4e208ee1e99a76fc424a |
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| Source note | uspto-grants-2012_12 |
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